Variant report

Variant	nsv975416
Chromosome Location	chr12:48882416-48893049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:123)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:48882861-48883157	GM12878	blood:	n/a	chr12:48883023-48883034
2	BATF	chr12:48884069-48884434	GM12878	blood:	n/a	n/a
3	BATF	chr12:48882829-48883217	GM12878	blood:	n/a	chr12:48883023-48883034
4	BCL11A	chr12:48882852-48883267	GM12878	blood:	n/a	n/a
5	BCLAF1	chr12:48882751-48883247	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:48882898-48883195	GM12878	blood:	n/a	n/a
7	CEBPB	chr12:48882593-48883325	GM12878	blood:	n/a	n/a
8	CTCF	chr12:48886780-48886930	NHLF	lung:	n/a	n/a
9	CUX1	chr12:48884595-48884647	GM12878	blood:	n/a	n/a
10	E2F4	chr12:48882935-48883203	MCF10A-Er-Src	breast:	n/a	n/a
11	EBF1	chr12:48884085-48884398	GM12878	blood:	n/a	n/a
12	EBF1	chr12:48882812-48883124	GM12878	blood:	n/a	chr12:48882931-48882942
13	EBF1	chr12:48882732-48883206	GM12878	blood:	n/a	chr12:48882931-48882942
14	EP300	chr12:48882788-48883206	GM12878	blood:	n/a	n/a
15	EP300	chr12:48882814-48883236	GM12878	blood:	n/a	n/a
16	FOS	chr12:48882823-48883213	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr12:48882825-48883232	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr12:48882762-48883225	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:48882837-48883421	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXM1	chr12:48882633-48883283	GM12878	blood:	n/a	n/a
21	IRF4	chr12:48882820-48883124	GM12878	blood:	n/a	n/a
22	IRF4	chr12:48882807-48883262	GM12878	blood:	n/a	n/a
23	MYC	chr12:48882797-48883582	MCF10A-Er-Src	breast:	n/a	n/a
24	MYC	chr12:48882824-48883500	MCF10A-Er-Src	breast:	n/a	n/a
25	NFIC	chr12:48882423-48883336	GM12878	blood:	n/a	n/a
26	POLR2A	chr12:48889038-48889116	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr12:48882470-48882524	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr12:48882749-48883524	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr12:48886005-48886242	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr12:48884670-48884745	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr12:48883021-48883149	MCF10A-Er-Src	breast:	n/a	n/a
32	RUNX3	chr12:48883878-48884459	GM12878	blood:	n/a	n/a
33	RUNX3	chr12:48882700-48883303	GM12878	blood:	n/a	n/a
34	RUNX3	chr12:48882835-48883231	GM12878	blood:	n/a	n/a
35	RUNX3	chr12:48884027-48884396	GM12878	blood:	n/a	n/a
36	SP1	chr12:48882811-48883134	GM12878	blood:	n/a	n/a
37	SP1	chr12:48882789-48883194	GM12878	blood:	n/a	n/a
38	SPI1	chr12:48885297-48885411	K562	blood:	n/a	n/a
39	SRF	chr12:48882983-48883111	GM12878	blood:	n/a	chr12:48883067-48883080 chr12:48883069-48883078 chr12:48883068-48883082 chr12:48883068-48883079
40	SRF	chr12:48882885-48883223	GM12878	blood:	n/a	chr12:48883067-48883080 chr12:48883069-48883078 chr12:48883068-48883082 chr12:48883068-48883079
41	SRF	chr12:48882914-48883195	GM12878	blood:	n/a	chr12:48883067-48883080 chr12:48883069-48883078 chr12:48883068-48883082 chr12:48883068-48883079
42	STAT3	chr12:48882822-48883227	MCF10A-Er-Src	breast:	n/a	n/a
43	STAT3	chr12:48882874-48883143	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr12:48882800-48883232	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr12:48882896-48883192	GM12878	blood:	n/a	n/a
46	STAT3	chr12:48882896-48883206	MCF10A-Er-Src	breast:	n/a	n/a
47	TBP	chr12:48882671-48883205	GM12878	blood:	n/a	n/a
48	WRNIP1	chr12:48886688-48886709	GM12878	blood:	n/a	n/a
49	ZNF143	chr12:48882852-48883158	GM12878	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48889853-48889903	NHDF-neo	bronchial:	n/a
2	chr12:48889853-48889903	NHDF-neo	bronchial:	n/a
3	chr12:48889853-48889903	NT2-D1	testis:	n/a
4	chr12:48884922-48884972	SKMC	muscle:	n/a
5	chr12:48889853-48889903	HIPEpiC	eye:	n/a
6	chr12:48889853-48889903	A549	lung:	n/a
7	chr12:48889853-48889903	HRPEpiC	eye:	n/a
8	chr12:48884922-48884972	HUVEC	blood vessel:	n/a
9	chr12:48889853-48889903	NHBE	bronchial:	n/a
10	chr12:48884922-48884972	H1-hESC	embryonic stem cell:	embryo
11	chr12:48884922-48884972	PrEC	prostate:	n/a
12	chr12:48889853-48889903	NH-A	brain:	n/a
13	chr12:48884922-48884972	HAEpiC	amniotic membrane:	n/a
14	chr12:48884922-48884972	Hepatocyte	liver:	n/a
15	chr12:48884922-48884972	T-47D	breast:	n/a
16	chr12:48889853-48889903	GM06990	blood:	n/a
17	chr12:48889853-48889903	HRE	kidney:	n/a
18	chr12:48884922-48884972	A549	lung:	n/a
19	chr12:48884922-48884972	GM12878	blood:	n/a
20	chr12:48889853-48889903	SKMC	muscle:	n/a
21	chr12:48889853-48889903	HCPEpiC	choroid plexus:	n/a
22	chr12:48889853-48889903	HUVEC	blood vessel:	n/a
23	chr12:48889853-48889903	MCF10A-Er-Src	breast:	n/a
24	chr12:48889853-48889903	HCF	heart:	n/a
25	chr12:48884922-48884972	MCF-7	breast:	n/a
26	chr12:48884922-48884972	Caco-2	colon:	n/a
27	chr12:48884922-48884972	AG09309	skin:	n/a
28	chr12:48884922-48884972	GM06990	blood:	n/a
29	chr12:48884922-48884972	U87	brain:	n/a
30	chr12:48889853-48889903	K562	blood:	n/a
31	chr12:48884922-48884972	HEEpiC	esophagus:	n/a
32	chr12:48889853-48889903	GM12891	blood:	n/a
33	chr12:48889853-48889903	ECC-1	luminal epithelium:	n/a
34	chr12:48884922-48884972	AG04450	lung:	fetal
35	chr12:48884922-48884972	ovcar-3	ovarian:	n/a
36	chr12:48884922-48884972	NHDF-neo	bronchial:	n/a
37	chr12:48889853-48889903	U87	brain:	n/a
38	chr12:48884922-48884972	HRCEpiC	kidney:	n/a
39	chr12:48884922-48884972	Hela-S3	cervix:	n/a
40	chr12:48884922-48884972	HCT-116	colon:	n/a
41	chr12:48889853-48889903	PANC-1	pancreas:	n/a
42	chr12:48884922-48884972	SK-N-SH_RA	brain:	n/a
43	chr12:48889853-48889903	ProgFib	skin:	n/a
44	chr12:48884922-48884972	BE2_C	brain:	n/a
45	chr12:48889853-48889903	T-47D	breast:	n/a
46	chr12:48889853-48889903	BE2_C	brain:	n/a
47	chr12:48889853-48889903	AG09309	skin:	n/a
48	chr12:48889853-48889903	SK-N-SH_RA	brain:	n/a
49	chr12:48889853-48889903	HL-60	blood:	n/a
50	chr12:48889853-48889903	AoSMC	blood vessel:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:48880500..48882865-chr12:48883478..48886344,3	K562	blood:
2	chr12:48877425..48880282-chr12:48884726..48886278,2	MCF-7	breast:
3	chr12:48888880..48891853-chr12:48895392..48897603,2	MCF-7	breast:
4	chr12:48887538..48890353-chr12:48917589..48920002,2	K562	blood:
5	chr12:48882871..48884702-chr12:48885100..48887755,2	K562	blood:
6	chr12:48887453..48890090-chr12:48892571..48894412,2	MCF-7	breast:
7	chr12:48880029..48882865-chr12:48884102..48887272,3	K562	blood:
8	chr12:48887453..48890090-chr12:48892571..48894412,2	MCF-7	breast:
9	chr12:48880500..48882865-chr12:48883478..48886344,3	K562	blood:
10	chr12:48882871..48884702-chr12:48885100..48887755,2	K562	blood:
11	chr12:48880029..48882865-chr12:48884102..48887272,3	K562	blood:
12	chr12:48875260..48877080-chr12:48883909..48886028,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR8S1-2	chr12:48888581-48888762	NONHSAT028007
2	lnc-OR8S1-2	chr12:48889964-48890169	NONHSAT028007
3	lnc-OR8S1-2	chr12:48886677-48886778	NONHSAT028007

No data

Variant related genes	Relation type
C12orf54	TF binding region
C12orf54	CpG island
ENSG00000197376	chromatin interactions
ENSG00000240443	chromatin interactions
ENSG00000177627	chromatin interactions

Extended variants
information (count: 407 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187356941	chr12:48882424-48882425	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs533619834	chr12:48882437-48882438	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145158565	chr12:48882440-48882441	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs549983112	chr12:48882515-48882516	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs569846254	chr12:48882532-48882533	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535420820	chr12:48882541-48882542	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2705126	chr12:48882562-48882563	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs567966329	chr12:48882563-48882564	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs533842857	chr12:48882588-48882589	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554078127	chr12:48882595-48882596	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201188992	chr12:48882662-48882663	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368968008	chr12:48882692-48882693	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371373533	chr12:48882726-48882727	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs140626422	chr12:48882727-48882728	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs374816095	chr12:48882754-48882755	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs142410491	chr12:48882760-48882761	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375262710	chr12:48882761-48882762	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs367910045	chr12:48882762-48882763	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200302287	chr12:48882774-48882775	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs369170617	chr12:48882785-48882786	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144943203	chr12:48882815-48882816	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576223126	chr12:48882831-48882832	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200088977	chr12:48882853-48882854	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561672754	chr12:48882904-48882905	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376207526	chr12:48882911-48882912	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs572738575	chr12:48882921-48882922	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200901187	chr12:48882943-48882944	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs73298787	chr12:48882966-48882967	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs564826890	chr12:48883000-48883001	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2705127	chr12:48883012-48883013	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs2731096	chr12:48883020-48883021	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs149045798	chr12:48883029-48883030	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs143004237	chr12:48883049-48883050	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs548923950	chr12:48883053-48883054	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs112381252	chr12:48883110-48883111	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111840037	chr12:48883119-48883120	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs535065864	chr12:48883173-48883174	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190977744	chr12:48883174-48883175	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs200739829	chr12:48883208-48883209	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370397633	chr12:48883209-48883210	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs56968979	chr12:48883225-48883226	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs182756388	chr12:48883287-48883288	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs35342454	chr12:48883301-48883302	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548974799	chr12:48883302-48883303	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140377696	chr12:48883308-48883309	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs2731097	chr12:48883311-48883312	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556347734	chr12:48883342-48883343	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537974979	chr12:48883381-48883382	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs576162553	chr12:48883396-48883397	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188122959	chr12:48883406-48883407	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48881000-48882800	Enhancers	NHEK	skin
2	chr12:48881600-48883800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:48881600-48884000	Enhancers	HMEC	breast
4	chr12:48882200-48882600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:48882400-48882600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:48882400-48884000	Enhancers	GM12878-XiMat	blood
7	chr12:48882600-48883000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:48882600-48883600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:48882800-48883200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:48882800-48883400	Flanking Active TSS	NHEK	skin
11	chr12:48883000-48883200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:48883200-48884000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:48883400-48884000	Enhancers	NHEK	skin
14	chr12:48883600-48883800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:48883800-48885200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:48884000-48884200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr12:48887000-48891800	Weak transcription	Brain Hippocampus Middle	brain
18	chr12:48887600-48890000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr12:48888000-48888600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr12:48888400-48888600	Weak transcription	Spleen	Spleen
21	chr12:48888600-48888800	ZNF genes & repeats	Spleen	Spleen
22	chr12:48888800-48891000	Weak transcription	Spleen	Spleen

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